Disease Browser
Parent Node: congenital anemia (MONDO:0000577) Parent Node: conjunctival tumor (MONDO:0020204) Parent Node: epidermal appendage tumor (MONDO:0002297) Parent Node: excretory apparatus of the lacrimal system anomaly (MONDO:0020195) Parent Node: hematopoietic and lymphoid system neoplasm (MONDO:0002334) Parent Node: hereditary eye tumor (MONDO:0015966) Parent Node: hereditary neoplastic syndrome (MONDO:0015356) Parent Node: hereditary poikiloderma (MONDO:0016382) Parent Node: hyperpigmentation of the skin (MONDO:0019289) Parent Node: inherited aplastic anemia (MONDO:0001713) Parent Node: inherited skin tumor (MONDO:0015950) Parent Node: malformation syndrome with hamartosis (MONDO:0020063) Parent Node: syndrome with combined immunodeficiency (MONDO:0018035) ..Starting node .. dyskeratosis congenita () Child Nodes:
........autosomal recessive dyskeratosis congenita 4 () ........dyskeratosis congenita, autosomal dominant 1 () ........dyskeratosis congenita, autosomal dominant 2 () ........dyskeratosis congenita, autosomal dominant 3 () ........dyskeratosis congenita, autosomal dominant 6 () ........dyskeratosis congenita, autosomal recessive 1 () ........dyskeratosis congenita, autosomal recessive 2 () ........dyskeratosis congenita, autosomal recessive 3 () ........dyskeratosis congenita, autosomal recessive 5 () ........dyskeratosis congenita, autosomal recessive 6 () ........dyskeratosis congenita, X-linked () ........Revesz syndrome () Sister Nodes: ..absent thumb-short stature-immunodeficiency syndrome () ..anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome () ..autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis () ..combined immunodeficiency due to CRAC channel dysfunction () ..combined immunodeficiency with faciooculoskeletal anomalies () ..DNA repair defect other than combined T-cell and B-cell immunodeficiencies () ..dyskeratosis congenita () ..facial dysmorphism-immunodeficiency-livedo-short stature syndrome () ..Hennekam syndrome () ..hepatic veno-occlusive disease-immunodeficiency syndrome () ..hereditary folate malabsorption () ..hyper-IgE syndrome () ..hypohidrotic ectodermal dysplasia with immunodeficiency () ..immuno-osseous dysplasia () ..immunodeficiency due to absence of thymus () ..Laron syndrome with immunodeficiency () ..multiple intestinal atresia () ..pancytopenia due to IKZF1 mutations () ..primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency () ..T-cell immunodeficiency, congenital alopecia, and nail dystrophy () ..transcobalamin II deficiency () ..Vici syndrome () ..Wiskott-Aldrich syndrome () MONDO is developed by the Monarch Initiative . Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM ,ClinVar , CTD